Survival and quality-of-life in mucormycosis: a multicentric ambispective cohort study.

Objectives: We aimed to evaluate long-term survival and identify predictors of mortality among patients hospitalized with mucormycosis.

Methods: This prospective, multicentre cohort study included patients hospitalized for mucormycosis across 26 sites in India from March to July 2021. Follow-up data were collected at 1-, 3-, 6-, and 12-month intervals post-discharge through telephonic or in-person interviews with patients or caregivers.

Recent Trend of Surge in Pulmonary involvement in Sinonasal Mucormycosis: A Case Series: Pulmonary involvement in Sinonasal Mucormycosis.

Mucormycosis is an angio-invasive fungal infection affecting individuals with immuno-compromised state. The case series is a retrospective analysis of patients in a single centre and highlights the surge of pulmonary involvement in patients with sinonasal mucormycosis. To determine incidence of sequential pulmonary involvement in diagnosed cases of sino-nasal mucormycosis undergoing treatment in a tertiary health care facility and devise institutional algorithm for management.

Giant Parathyroid Adenoma Causing Dyspnea: A Rare Clinical Presentation.

Primary hyperparathyroidism is an endocrine disorder with muti-system involvement. The clinical condition is dealt by multi-speciality department. Parathyroid adenoma is the principal cause of primary hyperparathyroidism.

Comparative Study of Inlay and Overlay Cartilage Perichondrium Composite Graft Myringoplasty.

Unlabelled: To compare results of inlay and overlay cartilage-perichondrium composite graft myringoplasty. The present study was conducted in the department of otorhinolaryngology, Pt. B.

Cytological and histopathological features of recurrent calcifying aponeurotic fibroma of neck in an adolescent male-rare presentation of a rare tumour.

Calcifying aponeurotic fibroma is a rare benign but locally aggressive soft tissue tumour. It is most commonly seen in distal extremities and very rarely seen in head and neck region. In this case report, we describe both cytological and histological features of this tumour in a young adolescent male.

Osteitis Fibrosis Cystica: Classical Case Report of an Uncommon Presentation in a Young Female.

Osteitis fibrosa cystica (OFC) is a skeletal disease related to long standing, end-stage hyperparathyroidism. However, nowadays hypercalcemia due to primary or secondary hyperparathyroidism can often be detected early by laboratory screening and imaging modalities; consequentially the frequency of osteitis fibrosa cystica has drastically declined. OFC, also termed as Brown tumor, can mimic primary bone tumors clinically, which often leads to misdiagnosis and inappropriate management.